Trial Review

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Trial registered on ANZCTR


Registration number
ACTRN12622000684729
Ethics application status
Approved
Date submitted
13/04/2022
Date registered
11/05/2022
Date last updated
3/10/2023
Date data sharing statement initially provided
11/05/2022
Type of registration
Prospectively registered

Titles & IDs
Public title
ECMT-154™ for the Topical Treatment of Eczema in Children
Scientific title
Randomised Controlled Trial of ECMT-154™ vs Vehicle Control for the Topical Treatment of Eczema in Children aged 2-12 YO
Secondary ID [1] 306813 0
MBS03
Universal Trial Number (UTN)
u1111-1275-6008
Trial acronym
Linked study record


Health condition
Health condition(s) or problem(s) studied:
Eczema 325895 0
Condition category
Condition code
Skin 323202 323202 0 0
Dermatological conditions

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Manuka-oil based 2% ECMT-154™ cream is applied topically, twice daily (morning and night) for 6 weeks. The amount required will be dependent on the individual child's eczema spread, with the participants' parent/guardian recommended to apply the treatment liberally to their eczema areas. A weekly participant diary will used by the participants' parent/guardian to monitor adherence, adverse events and to capture photographs of the representative eczema lesion.
Composition Ingredients: Propylene Glycol, Sodium lauryl sulfate, Stearyl alcohol, water, White soft paraffin, PEG 3350, PEG 300, 2% ECMT-154
Intervention code [1] 323278 0
Treatment: Drugs
Comparator / control treatment
Vehicle Control
Contains the same ingredients as the active intervention without the 2% ECMT-154™.
Participants' parents and guardians will be advised to follow the same treatment application as the 2% ECMT-154™ study treatment cream. A weekly participant diary will used by the participants' parent/guardian to monitor adherence, adverse events and to capture photographs of the representative eczema lesion.
Composition Ingredients include: Propylene Glycol, Sodium lauryl sulfate, Stearyl alcohol, water, White soft paraffin, PEG 3350, PEG 300
Control group
Placebo

Outcomes
Primary outcome [1] 330956 0
Difference in Patient Orientated Eczema Measure (POEM for proxy completion) scores
Timepoint [1] 330956 0
Baseline. Week 6 post-intervention commencement
Secondary outcome [1] 408245 0
Proportion of participants with a >=4 change in POEM score compared to baseline.
Timepoint [1] 408245 0
Baseline, Week 3 and 6 post-intervention commencement.
Secondary outcome [2] 408251 0
Difference in POEM scores at Week Six analysed per protocol
Timepoint [2] 408251 0
Week 3 and Week 6 post-intervention commencement.
Secondary outcome [3] 408252 0
Difference in PO-SCORAD score, assessing patient reported severity of eczema.
Timepoint [3] 408252 0
Week 3 and Week 6 post-intervention commencement.
Secondary outcome [4] 408253 0
Difference in dermatologist rated SCORAD score, clinical assessment of severity of eczema.
Timepoint [4] 408253 0
Week 6 post-intervention commencement.
Secondary outcome [5] 408254 0
The proportion of withdrawals will be assessed by audit of study records and through statistical analysis of estimation of relative risk.
Timepoint [5] 408254 0
Weekly up to Week 6 post-intervention commencement.
Secondary outcome [6] 408676 0
Proportion of treatment escalation between groups. Treatment escalation will be assessed initially by patient-reported via diary entry and then will be remotely assessed and documented by the MRINZ study doctor.
Timepoint [6] 408676 0
Weekly up to Week 6 post-intervention commencement.
Secondary outcome [7] 408677 0
Change in Children's Dermatology Life Quality Index (CDLQI) score for participants aged 4-12 years compared to baseline.
Timepoint [7] 408677 0
Baseline, Week 3 and Week 6 post-intervention commencement.
Secondary outcome [8] 408678 0
Acceptability of ECMT-154 in the treatment of eczema, rated in Numerical Rating Scale score (1 unacceptable to 10 acceptable)
Timepoint [8] 408678 0
Week 6 post-intervention commencement.
Secondary outcome [9] 408679 0
Proportions of cutaneous and systemic events between treatment groups. Will be classified as adverse events (AEs), these will initially be patient reported via diary entry and will then be remotely assessed and documented by the study doctor and if required the study dermatologist. All AE clinical outcomes will be recorded in the study CDMA and will be analysed and presented as an estimation of relative risk.
Timepoint [9] 408679 0
Week 6 post-intervention commencement.
Secondary outcome [10] 408680 0
Comparison of eczema intensity SCORAD scores (Part B) between blinded pharmacists to assess inter-rater variability of scoring.
Timepoint [10] 408680 0
Baseline and Week 6 post-intervention commencement.
Secondary outcome [11] 408681 0
Comparison of eczema intensity SCORAD scores (Part B) between blinded pharmacists and a blinded dermatologist to assess inter-rater variability of scoring.
Timepoint [11] 408681 0
Baseline and Week 6 post-intervention commencement.
Secondary outcome [12] 408682 0
Ability to use the participant taken photographs for AE review as assessed by a MRINZ Investigator using a numerical rating scale (1 unacceptable - 10 acceptable).
Timepoint [12] 408682 0
Week 3 post-intervention commencement
Secondary outcome [13] 408683 0
Ability to use participant taken photographs for clinical assessment scoring by teledermatology on numerical rating scale (1 unacceptable to 10 acceptable).
Timepoint [13] 408683 0
Week 3 post-intervention commencement only
Secondary outcome [14] 409286 0
Change in Infants' Dermatitis Quality of Life (IDQOL) score for participants aged 2-4 years compared to baseline.
Timepoint [14] 409286 0
Baseline, week 3, and week 6 post-intervention commencement

Eligibility
Key inclusion criteria
- Willing and able to provide written informed consent (parent/guardian) and assent (for participants aged 5-12 years)
- Participant is aged between 2 and 12 years of age, inclusive
- Parent/guardian reported, doctor diagnosis of eczema
- Patient has a representative eczema lesion, located below the clavicle that is in an area they are comfortable to have photographed.
- Patient has a POEM score of ‘moderate to severe eczema’ (8 to 24)
- Participant and parent/guardian are willing to stop all moisturisers and other skin barrier cream or emulsion used on participant during the treatment period and replace it with the investigational
product assigned in this trial. Usual facial regimens and application of sunscreen is permitted.
- Participant and parent/guardian are willing to replace participants body wash/soap with aqueous cream as supplied at enrolment.
- Participant and their parent/guardian are able to attend a follow up visit 6 weeks after they enroll in the study. This will take place at a participating pharmacy or via telephone call if required due to COVID restrictions or unanticipated inability to attend in person.
- Participant and their parent/guardian are willing and able to complete the study and comply with all study instructions.
- Parent/guardian must have internet access and ability to take a once weekly photograph of the representative eczema lesion for completing the online study diaries.
Minimum age
2 Years
Maximum age
12 Years
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
- Current requirement for prescription of antibiotics or corticosteroids for the treatment of any condition (with the exception of in and intranasal corticosteroids)
- Use of antihistamines, antibiotics or corticosteroids within the last two weeks (with the exception of inhaled and intranasal corticosteroids)
- Use of immunomodulatory medications taken for eczema within the last four weeks
- Use of bleach baths within the past seven days.
- Cutaneous mycotic or bacterial disease requiring a topical or systemic therapy
- Other skin condition which may affect the assessment of eczema
- History of allergy or hypersensitivity to study treatment ingredients
- Participation in a clinical study involving an investigational product during the last three months.
- Current cold/flu like symptoms, fever, or unexplained shortness of breath..
- Any other condition which, at the investigators’ discretion, is believed may present a safety risk or impact upon the ability of the
participant to complete the study.

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Randomisation of participants takes place at the pharmacy, electronically within REDCap, during visit one. Participants will first be randomised 1:1 to receive either the investigational treatment or vehicle control. Investigators will not have access to the randomisation schedule. Investigational product and active control will be dispensed in matching plain packaging
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
A statistician generated block randomisation schedule, using a block size of four, will be uploaded by an unblinded member of the MRINZ informatics team to the REDCap randomisation module.
Masking / blinding
Blinded (masking used)
Who is / are masked / blinded?



The people analysing the results/data
Intervention assignment
Parallel
Other design features
This study is considered to be single-blind, with central investigators unaware of treatment allocation. Participants are not advised of their treatment allocation. However, they are considered potentially unblinded due to the distinctive smell of the IMP.
Phase
Phase 2
Type of endpoint/s
Safety/efficacy
Statistical methods / analysis
No power calculation for sample size is required for this pilot. However, enrolling 50 patients total (25 in each arm) will provide reasonable precision based on between 20 and 25 degrees of freedom for chi-squared based estimation of standard deviation within each arm.

Recruitment
Recruitment status
Completed
Date of first participant enrolment
Anticipated
18/07/2022
Actual
2/08/2022
Date of last participant enrolment
Anticipated
1/04/2023
Actual
18/07/2023
Date of last data collection
Anticipated
1/06/2023
Actual
13/09/2023
Sample size
Target
50
Accrual to date
Final
50
Recruitment outside Australia
Country [1] 24697 0
New Zealand
State/province [1] 24697 0
Wellington

Funding & Sponsors
Funding source category [1] 311149 0
Commercial sector/Industry
Name [1] 311149 0
Manuka Biosciences
Country [1] 311149 0
New Zealand
Primary sponsor type
Commercial sector/Industry
Name
Manuka Biosciences
Address
Manuka Biosciences
300 Richmond Road,
Grey Lynn, Auckland, 1021
Country
New Zealand
Secondary sponsor category [1] 312498 0
None
Name [1] 312498 0
Address [1] 312498 0
Country [1] 312498 0

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 310677 0
Central Health and Disability Ethics Committee (HDEC)
Ethics committee address [1] 310677 0
Ethics committee country [1] 310677 0
New Zealand
Date submitted for ethics approval [1] 310677 0
13/04/2022
Approval date [1] 310677 0
30/06/2022
Ethics approval number [1] 310677 0
HDEC Review Reference: 2022 FULL 12496

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 118482 0
Dr Gabby Shortt
Address 118482 0
Medical Research Institute of New Zealand,
Level 7 Clinical Services Building,
Wellington Hospital,
Riddiford Street, Newtown
Wellington, 6021
Country 118482 0
New Zealand
Phone 118482 0
+64 4 805 0261
Fax 118482 0
Email 118482 0
[email protected]
Contact person for public queries
Name 118483 0
Gabby Shortt
Address 118483 0
Medical Research Institute of New Zealand,
Level 7 Clinical Services Building,
Wellington Hospital,
Riddiford Street, Newtown
Wellington, 6021
Country 118483 0
New Zealand
Phone 118483 0
+64 4 805 0261
Fax 118483 0
Email 118483 0
[email protected]
Contact person for scientific queries
Name 118484 0
Gabby Shortt
Address 118484 0
Medical Research Institute of New Zealand,
Level 7 Clinical Services Building,
Wellington Hospital,
Riddiford Street, Newtown
Wellington, 6021
Country 118484 0
New Zealand
Phone 118484 0
+64 4 805 0261
Fax 118484 0
Email 118484 0
[email protected]

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
No/undecided IPD sharing reason/comment
IPD sharing will not occur due to the nature of the pediatric assent procedures and pilot study status.


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

Documents added manually
No documents have been uploaded by study researchers.

Documents added automatically
No additional documents have been identified.